Global Labelling Director, Neuroscience Strategy

Novartis Farmacéutica; Dublin; Hybrid; EUR 90,300 - 167,700; Full time

Job summary

Novartis seeks a Global Labelling Director, Content to shape the global labelling strategy for neuroscience medicines. You will translate complex data into compliant, compelling product information and influence regulatory decisions across markets.

You will lead cross‑functional collaborations with regulatory, clinical, safety, medical and commercial teams to align strategies, negotiate with health authorities, and uphold quality and compliance standards in a global matrix environment.

Qualifications

• Significant experience in global labelling or regulatory affairs within the pharmaceutical industry.
• Proven ability to lead labelling strategy for complex development and lifecycle products.
• Strong understanding of drug development, benefit‑risk assessment and safety data interpretation.
• Excellent cross‑functional stakeholder influence within a global matrix.

Responsibilities

• Lead global labelling content strategies for neuroscience assets, ensuring alignment with product and regulatory objectives.
• Drive development of core and major market labelling, including global and regional prescribing information.
• Shape key product claims and positions using scientific evidence and regulatory insight.
• Partner across regulatory, clinical, safety, medical and commercial teams to achieve global alignment.
• Lead interactions and negotiations on labelling content with health authorities when required.
• Monitor regulatory developments and competitor intelligence to strengthen labelling strategies and market positioning.
• Champion quality, compliance and capability building through coaching and knowledge sharing.

Skills

Strategic leadership

Regulatory affairs

Cross-functional collaboration

Communication skills

Decision-making

Education

Advanced life sciences degree

Job description

Novartis seeks a Global Labelling Director, Content to shape the global labelling strategy for neuroscience medicines. You will translate complex data into compliant, compelling product information and influence regulatory decisions across markets.

You will lead cross‑functional collaborations with regulatory, clinical, safety, medical and commercial teams to align strategies, negotiate with health authorities, and uphold quality and compliance standards in a global matrix environment.